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1.
Genes Cells ; 25(8): 582-592, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32516841

ABSTRACT

Collective cell migration, in which cells assemble and move together, is an essential process in embryonic development, wound healing and cancer metastasis. Chemokine signaling guides cell assemblies to their destinations. In zebrafish posterior lateral line primordium (PLLP), a model system for collective cell migration, it has been proposed that the chemokine ligand Cxcl12a secreted from muscle pioneer cells (MPs) and muscle fast fibers (MFFs), which are distributed along with the horizontal midline, binds to the receptor Cxcr4b in PLLP and that Cxcl12a-Cxcr4b signaling guides the anterior-to-posterior migration of PLLP along the horizontal midline. However, how the surrounding tissues affect PLLP migration remains to be elucidated. Here, we investigated the relationship between the PLLP and the surrounding tissues and found that a furrow between the dorsal and ventral myotomes is generated by Sonic hedgehog (Shh) signaling-dependent MP and MFF differentiation and that the PLLP migrates in this furrow. When transient inhibition of Shh signaling impaired both the furrow formation and differentiation of cxcl12a-expressing MPs/MFFs, directional PLLP migration was severely perturbed. Furthermore, when differentiated MPs and MFFs were ablated by femtosecond laser irradiations, the furrow remained and PLLP migration was relatively unaffected. These results suggest that the furrow formation between the dorsal and ventral myotomes is associated with the migratory behavior of PLLP.


Subject(s)
Cell Movement/physiology , Lateral Line System/embryology , Zebrafish/embryology , Animals , Cell Cycle/genetics , Cell Differentiation/genetics , Chemokine CXCL12/metabolism , Embryonic Development , Gene Expression Regulation, Developmental , Hedgehog Proteins/metabolism , Receptors, CXCR4/metabolism , Signal Transduction/genetics , Zebrafish/metabolism , Zebrafish Proteins/metabolism
2.
Cell Rep ; 27(3): 928-939.e4, 2019 04 16.
Article in English | MEDLINE | ID: mdl-30995487

ABSTRACT

Establishment of robust gene expression boundary is crucial for creating elaborate morphology during development. However, mechanisms underlying boundary formation have been extensively studied only in a few model systems. We examined the establishment of zic1/zic4-expression boundary demarcating dorsoventral boundary of the entire trunk of medaka fish (Oryzias latipes) and identified a subgroup of dermomyotomal cells called horizontal boundary cells (HBCs) as crucial players for the boundary formation. Embryological and genetic analyses demonstrated that HBCs play crucial roles in the two major events of the process, i.e., refinement and maintenance. In the refinement, HBCs could serve as a chemical barrier against Wnts from the neural tube by expressing Hhip. At later stages, HBCs participate in the maintenance of the boundary by differentiating into the horizontal myoseptum physically inhibiting cell mixing across the boundary. These findings reveal the mechanisms underlying the dorsoventral boundary in the teleost trunk by specialized boundary cells.


Subject(s)
Fish Proteins/metabolism , Somites/metabolism , Transcription Factors/metabolism , Animals , Animals, Genetically Modified/metabolism , Body Patterning/genetics , Cell Differentiation , Chromosomes, Artificial, Bacterial/genetics , Fish Proteins/genetics , Gene Expression Regulation, Developmental , Oryzias/metabolism , Somites/cytology , Transcription Factors/genetics , Zebrafish/metabolism
3.
Dev Growth Differ ; 61(3): 252-262, 2019 Apr.
Article in English | MEDLINE | ID: mdl-30843193

ABSTRACT

The forebrain develops into the telencephalon, diencephalon, and optic vesicle (OV). The OV further develops into the optic cup, the inner and outer layers of which develop into the neural retina and retinal pigmented epithelium (RPE), respectively. We studied the change in fate of the OV by using embryonic transplantation and explant culture methods. OVs excised from 10-somite stage chick embryos were freed from surrounding tissues (the surface ectoderm and mesenchyme) and were transplanted back to their original position in host embryos. Expression of neural retina-specific genes, such as Rax and Vsx2 (Chx10), was downregulated in the transplants. Instead, expression of the telencephalon-specific gene Emx1 emerged in the proximal region of the transplants, and in the distal part of the transplants close to the epidermis, expression of an RPE-specific gene Mitf was observed. Explant culture studies showed that when OVs were cultured alone, Rax was continuously expressed regardless of surrounding tissues (mesenchyme and epidermis). When OVs without surrounding tissues were cultured in close contact with the anterior forebrain, Rax expression became downregulated in the explants, and Emx1 expression became upregulated. These findings indicate that chick OVs at stage 10 are bi-potential with respect to their developmental fates, either for the neural retina or for the telencephalon, and that the surrounding tissues have a pivotal role in their actual fates. An in vitro tissue culture model suggests that under the influence of the anterior forebrain and/or its surrounding tissues, the OV changes its fate from the retina to the telencephalon.


Subject(s)
Retina/embryology , Animals , Body Patterning/physiology , Cell Differentiation/physiology , Chick Embryo , Gene Expression Regulation, Developmental/physiology , Immunohistochemistry , Retina/cytology , Retina/metabolism , Retinal Pigments/metabolism , Telencephalon/cytology , Telencephalon/embryology , Telencephalon/metabolism
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